Towards a Global Cancer Knowledge Network: Dissecting the current international cancer genomic sequencing landscape
Vis D J, Lewin J, Liao RG, Mao M, Andre F, Ward RL, et al.. Towards a Global Cancer Knowledge Network: Dissecting the current international cancer genomic sequencing landscape. Annals of Oncology. 2017. [Epub ahead of print]

PathOS: a decision support system for reporting high throughput sequencing of cancers in clinical diagnostic laboratories
Doig KD, Fellowes A, Bell AH, Seleznev A, Ma D, Ellul J, et al. PathOS: a decision support system for reporting high throughput sequencing of cancers in clinical diagnostic laboratories. Genome medicine. 2017. 9 (1) : 38.

Germline variants in familial pituitary tumour syndrome genes are common in young patients and families with additional endocrine tumours
De Sousa SM, McCabe MJ, Wu K, Roscioli T, Gayevskiy V, Brook K, et al. Germline variants in familial pituitary tumour syndrome genes are common in young patients and families with additional endocrine tumours. European journal of endocrinology. 2017. 176 (5) : 635—644.

Case report of whole genome sequencing in the XY female: identification of a novel SRY mutation and revision of a misdiagnosis of androgen insensitivity syndrome
De Sousa SM, Kassahn KS, McIntyre LC, Chong CE, Scott HS, Torpy DJ. Case report of whole genome sequencing in the XY female: identification of a novel SRY mutation and revision of a misdiagnosis of androgen insensitivity syndrome. BMC Endocrine Disorders. 2016. 16 (1) : 58.

Targeted pharmacotherapy after somatic cancer mutation screening
Polasek TM, Ambler K, Scott HS, Sorich MJ, Kaub PA, Rowland A, et al. Targeted pharmacotherapy after somatic cancer mutation screening. F1000Research. 2016. 5 : 1551.